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MEETINGS / EVENTS

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January 23 - 25 2015, 12:00 AM - 12:00 AM

ASA PRACTICE MANAGEMENT 2015

February 07 - 08 2015, 12:00 AM - 12:00 AM

ASA Certificate in Business Administration 2015

June 26 - 28 2015, 12:00 AM - 12:00 AM

Annual Perioperative Surgical Home Summit

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FDA MEDWATCH ALERTS

December 18, 2014

0.9 Percent Sodium Chloride Injection USP in 100 mL MINI-BAG PLUS Container by Baxter: Recall - Particulate Matter

Summary:

FDA MedWatch Recall - Particulate Matter

November 21, 2014

FDA MedWatch - Respironics California, Esprit V1000 and V200 Ventilators: Class I Recall - Power Failure May Occur

Summary:

FDA MedWatch Respironics California Esprit V1000 and V200 Ventilators Class I Recall

November 21, 2014

FDA MedWatch - Highly Concentrated Potassium Chloride Injection, 10 mEq per 100 mL by Baxter: Recall - Mislabeled

Summary:

Highly Concentrated Potassium Chloride Injection 10 mEq per 100 mL by Baxter Recall Mislabeled

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Self-Education and Evaluation (SEE) Program

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New System for Patients to Report Medical Mistakes Concerns Lawmakers

Wednesday, October 03, 2012

In response to an article from the New York Times on a proposed new program that would allow patients to report on medical errors by health care providers to the federal government, a handful of physician lawmakers sent a letter to the Director of the Agency for Healthcare Research and Quality (AHRQ) Carolyn Clancy, M.D.s  registering concerns and posing a number of questions about the proposed policy. 

The letter was signed by Senators Tom Coburn (R-OK) and John Boozman (R-AR) and Representatives Bill Cassidy (R-LA), Ron Paul (R-TX), Phil Gingrey (R-GA), Paul Broun (R-GA), John Fleming (R-LA) and Phil Roe (R-TN).

Among other concerns, lawmakers point out that “many patients do not have the medical knowledge to accurately determine when an adverse medical event occurs.”

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